Have questions? Visit https://www.reddit.com/r/SNPedia

rs150239404

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs150239404(A;A)
Make rs150239404(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position100253422
GeneCWF19L1
is asnp
is mentioned by
dbSNPrs150239404
dbSNP (classic)rs150239404
ClinGenrs150239404
ebirs150239404
HLIrs150239404
Exacrs150239404
Gnomadrs150239404
Varsomers150239404
LitVarrs150239404
Maprs150239404
PheGenIrs150239404
Biobankrs150239404
1000 genomesrs150239404
hgdprs150239404
ensemblrs150239404
geneviewrs150239404
scholarrs150239404
googlers150239404
pharmgkbrs150239404
gwascentralrs150239404
openSNPrs150239404
23andMers150239404
23andMe allrs150239404
SNPshotrs150239404
SNPdbers150239404
MSV3drs150239404
GWAS Ctlgrs150239404
Max Magnitude0
ClinVar
Risk rs150239404(A;A)
Alt rs150239404(A;A)
Reference Rs150239404(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CWF19L1
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.102013179G>A
CLNSRC
CLNACC RCV000486185.1,